Weaver Syndrome: A Rare Cause of Neonatal Macrosomia and Dysmorphism. A Case Report.
Weaver syndrome is a rare genetic disorder characterized by abnormally excessive growth both in utero and postnatally. It is associated with a mutation in the EZH2 gene, which leads to accelerated bone development and other clinical manifestations such as macrocephaly, a characteristic dysmorphic...
সংরক্ষণ করুন:
| প্রধান লেখক: | , |
|---|---|
| বিন্যাস: | Artigo |
| ভাষা: | Árabe |
| প্রকাশিত: |
Algerian Society of Clinical & Oncological Pharmacy
2025-06-01
|
| মালা: | Batna Journal of Medical Sciences |
| বিষয়গুলি: | |
| অনলাইন ব্যবহার করুন: | https://batnajms.net/wp-content/uploads/Archives/2025/2/BJMS_Guellouh.pdf |
| ট্যাগগুলো: |
কোনো ট্যাগ নেই, প্রথমজন হিসাবে ট্যাগ করুন!
|